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口服 THC 给药后,在口服唾液中大麻素的处置情况。

Disposition of cannabinoids in oral fluid after controlled around-the-clock oral THC administration.

机构信息

Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, NIH, Baltimore, MD 21224, USA.

出版信息

Clin Chem. 2010 Aug;56(8):1261-9. doi: 10.1373/clinchem.2009.141853. Epub 2010 Jun 8.

Abstract

BACKGROUND

Oral fluid, a promising alternative matrix for drug monitoring in clinical and forensic investigations, offers noninvasive sample collection under direct observation. Cannabinoid distribution into oral fluid is complex and incompletely characterized due to the lack of controlled drug administration studies.

METHODS

To characterize cannabinoid disposition in oral fluid, we administered around-the-clock oral Delta(9)-tetrahydrocannabinol (THC) (Marinol) doses to 10 participants with current daily cannabis use. We obtained oral fluid samples (n=440) by use of Quantisal collection devices before, during, and after 37 20-mg THC doses over 9 days. Samples were extracted with multiple elution solvents from a single SPE column and analyzed by 2-dimensional GC-MS with electron-impact ionization for THC, 11-hydroxy-THC (11-OH-THC), cannabidiol, and cannabinol and negative chemical ionization for 11-nor-9-carboxy-THC (THCCOOH). Linear ranges were 0.5-50 microg/L, with the exception of cannabinol (1-50 microg/L) and THCCOOH (7.5-500 ng/L).

RESULTS

THCCOOH was the most prevalent analyte in 432 samples (98.2%), with concentrations up to 1117.9 ng/L. In contrast, 11-OH-THC was not identified in any sample; cannabidiol and cannabinol were quantified in 3 and 8 samples, respectively, with maximum concentrations of 2.1 and 13 microg/L. THC was present in only 20.7% of samples, with highest concentrations near admission (median 4.2 microg/L, range 0.6-481.9) from previously self-administered smoked cannabis.

CONCLUSIONS

Measurement of THCCOOH in OF not only identifies cannabis exposure, but also minimizes the possibility of passive inhalation. THCCOOH may be a better analyte for detection of cannabis use.

摘要

背景

唾液是一种有前途的替代基质,可用于临床和法医调查中的药物监测,它提供了在直接观察下进行非侵入性样本采集的方法。由于缺乏对照药物管理研究,因此大麻素在唾液中的分布情况很复杂,且尚未完全确定。

方法

为了描述唾液中大麻素的处置情况,我们对 10 名目前每日吸食大麻的参与者进行了 24 小时口服 Delta(9)-四氢大麻酚(Marinol)剂量给药。在 9 天内给予 37 次 20mg THC 剂量期间和之后,我们使用 Quantisal 收集装置获得了 440 份唾液样本。使用单个 SPE 柱进行多次洗脱溶剂提取,并通过二维 GC-MS 进行分析,采用电子轰击电离检测 THC、11-羟基-THC(11-OH-THC)、大麻二酚和大麻酚,采用负化学电离检测 11-去甲-9-羧基-THC(THCCOOH)。线性范围为 0.5-50μg/L,除大麻酚(1-50μg/L)和 THCCOOH(7.5-500ng/L)外。

结果

在 432 个样本中,最常见的分析物是 THCCOOH(98.2%),浓度高达 1117.9ng/L。相比之下,任何样本中均未检测到 11-OH-THC;3 个样本中定量了大麻二酚,8 个样本中定量了大麻酚,最高浓度分别为 2.1μg/L 和 13μg/L。只有 20.7%的样本中存在 THC,最高浓度出现在入院时(中位数 4.2μg/L,范围 0.6-481.9),这是先前自行吸食的吸食大麻。

结论

在 OF 中测量 THCCOOH 不仅可以识别大麻素暴露,还可以最大程度地减少被动吸入的可能性。THCCOOH 可能是检测大麻使用的更好分析物。

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